Flow focusing method and system for forming concentrated volumes of microbeads, and microbeads formed further thereto

ABSTRACT

In a method and system for forming concentrated volumes of microbeads, a polymer solution and/or suspension includes a polymer dissolved and/or dispersed in a medium. Streams of a focusing fluid and of the polymer solution and/or suspension flow towards a fluid bath, and into intersection with one another, so as to focus the polymer solution and/or suspension. The polymer solution and/or suspension stream forms microbeads in the fluid bath Some of the focusing fluid is drawn from the fluid bath, so as to concentrate the microbeads in the fluid bath. The system includes a flow focusing apparatus and a liquid-containing cell. The focusing apparatus includes polymer and focusing nozzles. The cell contains the fluid bath and has an outlet port, through which the focusing fluid is drawn.

RELATED APPLICATIONS

This is a divisional of U.S. patent application Ser. No. 12/682,710, filed on Dec. 13, 2010, currently pending, which is a U.S. national entry of PCT/CA2008/001808, filed on Oct. 10, 2008. PCT/CA2008/001808 claims the benefit of U.S. Provisional Application No. 60/979,667, filed Oct. 12, 2007. The disclosures of which are hereby incorporated by reference in their entirety.

FIELD OF THE INVENTION

The present invention relates generally to a method and system for forming microbeads, and more particularly, to a flow focusing method and system for forming concentrated volumes of microbeads, and to microbeads formed farther thereto.

BACKGROUND OF THE INVENTION

It may be preferable for large scale manufacture of microbeads (such as, for example, polymer microbeads) to allow for the control of various parameters. Some of these parameters may include, among others, control over: (i) bead diameter, (ii) degree of monodispersity, (iii) bead surface morphology and functionality, and/or (iv) rate of production—i.e., preferably, so as to enable a high-throughput.

The act of binding nanoparticles—such as quantum dots (QDs)—to polymer microbeads (e.g., for the use in diagnostic applications) may create additional manufacturing challenges and/or may increase the need for high quality, uniform and stable polymer beads. These and other potential uses for polymer microbeads may create a significant need for a large-scale method and system for forming same.

There is a known process for making polymer microbeads (or “microspheres” as they are sometimes called) which uses a flow focusing technique. Issued U.S. Pat. No. 6,116,516 (Ganan-Calvo) is illustrative in this regard. Heretofore, however, it may not have been readily apparent to those of ordinary skill in the art how one might adapt such flow focusing techniques to make polymer microbeads incorporating nanoparticles (e.g., in particular, QDs and/or magnetic nanoparticles), inter alia, in a one-step method. That is, known processes may not have been readily adaptable for use in association with the large-scale production of such polymer microbeads.

There may, therefore, exist a need for a novel method and system for large-scale manufacture of polymer microbeads.

Prior art flow focusing techniques may have been somewhat unsuitable for the manufacture of microbeads in large quantities (e.g., quantities of microbeads having a collective weight of several grams), perhaps in part because of the significant volume of ‘waste’ liquid used during the process. The significant amount of liquid previously used may have been due, to a great extent, on the substantial flow rate of the focusing liquid. It may be desirable to effectively address and creatively solve this problem—i.e., to deal with the large volumes of liquid previously used by flow focusing techniques for forming polymer microbeads—since it is one which may severely limit current production rates for microbeads. There may exist a need for a method and system for microbead manufacture which may minimize and/or reduce the amount of focusing fluid used, and/or which may afford greater control over the amount of focusing fluid produced.

A potentially serious concern arising from prior art microbead production methods may have been the generally low concentrations of microbeads so produced. Perhaps due in part to the volume of focusing liquid required in the prior art, microbeads may typically only be present in relatively low concentrations in product solutions (e.g., <0.02 wt %). Accordingly, for many microbead applications, additional steps (e.g., one or more centrifugation) may have been employed, on a more or less widespread basis, to bring the microbeads up to usable concentrations. In view thereof, there may exist a need for a method and system for forming, or manufacturing, microbeads at higher concentrations. Preferably, such a method or system would minimize, reduce or entirely eliminate any need to perform any additional concentrating steps.

It is, therefore, an object of one preferred embodiment according to the invention to provide a method and/or a system for fowling microbeads.

It is an object of one preferred embodiment according to the invention to provide a method and/or a system for forming polymer microbeads.

It is an object of one preferred embodiment according to the invention to provide a method and/or a system for large-scale and/or high-throughput manufacture of microbeads.

It is an object of one preferred embodiment according to the invention to provide a method and/or a system for forming microbeads which affords increased control over: (i) bead diameter, (ii) degree of monodispersity, (iii) bead surface morphology and functionality, and/or (iv) rate of production.

It is an object of one preferred embodiment according to the invention to provide a method and/or a system for large-scale manufacture of microbeads binding nanoparticles, such, as QDs.

It is an object of one preferred embodiment according to the invention to provide a method and/or a system for large-scale manufacture of high-quality, uniform and/or stable microbeads.

It is an object of one preferred embodiment according to the invention to provide a method and/or a system for large-scale manufacture of highly concentrated volumes of microbeads.

It is an object of one preferred embodiment according to the invention to provide a method and/or a system for large-scale manufacture of microbeads which reduces, minimizes and/or eliminates any need for subsequent centrifugation steps to concentrate same.

It is an object of one preferred embodiment according to the invention to provide a method and/or a system for large-scale flow focusing manufacture of microbeads which reduces and/or minimizes the amount of focusing fluid used, and/or which affords greater control over the amount of focusing fluid produced.

It is an object of one preferred embodiment according to the invention to provide a method and/or a system for large-scale flow focusing manufacture of microbeads, with the method and/or system being adapted to recycles at least some of the focusing fluid used.

It is an object of the present invention to obviate or mitigate one or more of the aforementioned disadvantages associated with the prior art, and/or to achieve one or more of the aforementioned objects of the invention.

SUMMARY OF THE INVENTION

According to the invention, there is disclosed a method of forming one or more concentrated volumes of microbeads. The method includes steps (a), (b), (c) and (d). In step (a) a focused stream of a polymer solution and/or suspension is flowed towards a fluid bath. The polymer solution and/or suspension includes a polymer dissolved and/or dispersed in a medium. In step (b), a focusing stream of a focusing fluid is flowed towards the fluid bath, and into intersection with the focused stream. In step (c), the focusing stream and the focused stream are flowed from intersection with one another, so as to the microbeads in the fluid bath. In step (d), a volume of the focusing fluid is flowed from the fluid bath, so as to concentrate the microbeads in the fluid bath.

According to an aspect of one preferred embodiment of the invention, preferably in step (d), the fluid bath may preferably, but need not necessarily, be controlled so as to be maintained at a substantially constant liquid level.

According to an aspect of one preferred embodiment of the invention, the substantially constant liquid level may preferably, but need not necessarily, be maintained by balancing respective flow rates for the focused stream in step (a), the focusing stream in step (b), and/or the focusing fluid in step (d).

According to an aspect of one preferred embodiment of the invention, preferably in step (d), the volume of the focusing fluid may preferably, but need not necessarily, flow through one or more filters.

According to an aspect of one preferred embodiment of the invention, preferably in step (d), the filters may preferably, but need not necessarily, retain the microbeads—preferably, in the fluid bath.

According to an aspect of one preferred embodiment of the invention, preferably in step (d), the filters may preferably, but need not necessarily, retain a substantially monodisperse set of the microbeads, preferably in the fluid bath.

According to an aspect of one preferred embodiment of the invention, preferably in step (d), the filters may preferably, but need not necessarily, divide the microbeads into one or more collections of microbeads. Each of the collections may preferably, but need not necessarily, include a respectively monodisperse set of the microbeads.

According to an aspect of one preferred embodiment of the invention, preferably at least one of steps (a) and (b) may preferably, but need not necessarily, be performed within an interior chamber of a flow focusing body.

According to an aspect of one preferred embodiment of the invention, steps (a) and (b) may preferably, but need not necessarily, be both performed within the interior chamber of the flow focusing body. An outlet portion of the flow focusing body may preferably, but need not necessarily, be located below a liquid level of the fluid bath. Preferably in step (c), the focusing stream and the focused stream may preferably, but need not necessarily, flow out from the outlet portion of the flow focusing body.

According to an aspect of one preferred embodiment of the invention, preferably in step (b), the focused stream may preferably, but need not necessarily, be focused by the focusing fluid. Preferably in step (c), the focusing stream and the focused stream may preferably, but need not necessarily, flow out from the outlet portion as a single flow stream.

According to an aspect of one preferred embodiment of the invention, preferably in step (c), the focusing stream may preferably, but need not necessarily, substantially surround the focused stream—preferably, in the single flow stream.

According to an aspect of one preferred embodiment of the invention, the method may preferably, but need not necessarily, also include a preliminary step, preferably before step (a), of providing the fluid bath within a sealed liquid-containing cell.

According to an aspect of one preferred embodiment of the invention, preferably at least one of steps (a) through (c) may preferably, but need not necessarily, be performed within the liquid-containing cell.

According to an aspect of one preferred embodiment of the invention, preferably in the preliminary step, the liquid-containing cell may preferably, but need not necessarily, additionally contain a volume of a gas, preferably at a predetermined pressure.

According to an aspect of one preferred embodiment of the invention, preferably in the preliminary step, a gas pressure source may preferably, but need not necessarily, pressurize the gas, preferably via an inlet valve, and preferably in the sealed liquid-containing cell.

According to an aspect of one preferred embodiment of the invention, the method may preferably, but need not necessarily, also include step (c.1), preferably after the preliminary step, of releasing a portion of the gas or the fluid bath, preferably via a pressure safety valve, and preferably when the pressure exceeds a predetermined maximum safety pressure for the sealed liquid-containing cell.

According to an aspect of one preferred embodiment of the invention, the gas may preferably, but need not necessarily, include an inert gas.

According to an aspect of one preferred embodiment of the invention, the pressure of the gas in the preliminary step may preferably, but need not necessarily, be predetermined—preferably, in balance with respective flow rates for the focused stream in step (a) and/or the focusing stream in step (b)—to maintain the fluid bath at a substantially constant liquid level.

According to an aspect of one preferred embodiment of the invention, the method may preferably, but need not necessarily, also include step (b.1), preferably after step (b), of maintaining the fluid bath under stirring. The microbeads may preferably, but need not necessarily, be allowed to solidify in step (c).

According to an aspect of one preferred embodiment of the invention, preferably in step (b.1), a stirring bar may preferably, but need not necessarily, maintain the fluid bath under stirring. The stirring bar may preferably, but need not necessarily, include an electric stirring bar or a magnetic stirring bar.

According to an aspect of one preferred embodiment of the invention, the method may preferably, but need not necessarily, also include step (d.1), preferably after step (d), wherein substantially solidified microbeads may preferably, but need not necessarily, be recovered from the fluid bath.

According to an aspect of one preferred embodiment of the invention, the method may preferably, but need not necessarily, also include step (e) of recycling at least part of the volume of the focusing fluid, preferably flowing from the fluid bath in step (d), and preferably as at least part of the focusing stream flowing into intersection with the focused stream in step (b).

According to an aspect of one preferred embodiment of the invention, preferably in step (a), the medium may preferably, but need not necessarily, include an organic solvent.

According to an aspect of one preferred embodiment of the invention, preferably in step (a), the polymer may preferably, but need not necessarily, be substantially hydrophobic.

According to an aspect of one preferred embodiment of the invention, preferably in step (a), the polymer may preferably, but need not necessarily, include a polystyrene powder and/or a derivative thereof.

According to an aspect of one preferred embodiment of the invention, preferably in step (b), the focusing fluid may preferably, but need not necessarily, include water.

According to an aspect of one preferred embodiment of the invention, preferably in step (a), the polymer solution and/or suspension may preferably, but need not necessarily, also include particles dissolved and/or dispersed in the medium. Preferably in step (c), each of the microbeads may preferably, but need not necessarily, bind an identifiable set of the particles.

According to an aspect of one preferred embodiment of the invention, preferably in step (a), the particles may preferably, but need not necessarily, include fluorophores.

According to an aspect of one preferred embodiment of the invention, preferably in step (a), the particles may preferably, but need not necessarily, include nanoparticles.

According to an aspect of one preferred embodiment of the invention, preferably in step (a), the particles may preferably, but need not necessarily, include quantum dots.

According to an aspect of one preferred embodiment of the invention, preferably in step (a), the particles may preferably, but need not necessarily, include a combination of quantum dots and/or magnetic nanoparticles.

According to an aspect of one preferred embodiment of the invention, preferably in step (a), the polymer solution and/or suspension may preferably, but need not necessarily, have a concentration of about 0.04 by weight-weight percentage (4 wt %).

According to the invention, there is also disclosed a microbead formed according to the method in any one of the above methods.

According to an aspect of one preferred embodiment of the invention, the microbead may preferably, but need not necessarily, include one or more functional groups at a surface thereof. The functional groups may preferably, but need not necessarily, be adapted to operatively bind with biorecognition molecules.

According to an aspect of one preferred embodiment of the invention, the microbead preferably, operatively bound with the biorecognition molecules—may preferably, but need not necessarily, be adapted for use as a probe, preferably in a multiplexed diagnostic test, and preferably for detection of one or more diseases.

According to an aspect of one preferred embodiment of the invention, the diseases may preferably, but need not necessarily, include malaria, HIV, Hepatitis B, Hepatitis C, Dengue virus, and/or avian flu (H5N1).

According to an aspect of one preferred embodiment of the invention, the microbead—preferably, operatively bound with the biorecognition molecules—may preferably, but need not necessarily, be adapted for use as a probe, preferably in a multiplexed diagnostic test, and preferably for detection of one or more genetic expression factors.

According to the invention, there is additionally disclosed a system for forming one or more concentrated volumes of microbeads. The system includes a fluid bath, a focusing fluid, and a polymer solution and/or suspension including a polymer dissolved and/or dispersed in a medium. The system also includes a flow focusing apparatus. The flow focusing apparatus includes a polymer nozzle and a focusing nozzle. The polymer nozzle operatively delivers a focused stream of the polymer solution and/or suspension. The focusing nozzle operatively delivers a focusing stream of the focusing solution. The flow focusing apparatus operatively delivers the focused stream and the focusing stream into intersection with one another. The flow focusing apparatus operatively flows the focusing stream and the focused stream into the fluid bath, so as to form the microbeads in the fluid bath. The system also includes a liquid-containing cell which is shaped to define an outlet port. The liquid-containing cell operatively contains the fluid bath. The liquid-containing cell operatively delivers a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath.

According to an aspect of one preferred embodiment of the invention, operative flow rates for (i) the focused stream through the polymer nozzle, (ii) the focusing stream through the focusing nozzle, and/or (iii) the focusing fluid through the outlet port, respectively, may preferably be predetermined—preferably in dependent relation upon one another, and preferably so as to maintain the fluid bath at a substantially constant liquid level.

According to an aspect of one preferred embodiment of the invention, the liquid-containing cell may preferably, but need not necessarily, include one or more filters—preferably, on the outlet port. The volume of the focusing fluid may preferably, but need not necessarily, be operatively delivered, through the filters, preferably out from the fluid bath.

According to an aspect of one preferred embodiment of the invention, the filters may preferably, but need not necessarily, operatively retain the microbeads—preferably, in the fluid bath.

According to an aspect of one preferred embodiment of the invention, the filters may preferably, but need not necessarily, retain a substantially monodisperse set of the microbeads—preferably, in the fluid bath.

According to an aspect of one preferred embodiment of the invention, the filters may preferably, but need not necessarily, operatively divide the microbeads into one or more collections of microbeads. Each of the collections may preferably, but need not necessarily, include a respectively monodisperse set of the microbeads.

According to an aspect of one preferred embodiment of the invention, the flow focusing apparatus may preferably, but need not necessarily, also include a flow focusing body. The flow focusing body may preferably, but need not necessarily, define an interior chamber and an outlet portion. The focused stream and the focusing stream may preferably, but need not necessarily, be operatively delivered into intersection with one another in the chamber. The focusing stream and the focused stream may preferably, but need not necessarily, operatively flow out from the outlet portion of the flow focusing body.

According to an aspect of one preferred embodiment of the invention, the outlet portion of the flow focusing body may preferably, but need not necessarily, be operatively located below a liquid level of the fluid bath.

According to an aspect of one preferred embodiment of the invention, the focused stream may preferably, but need not necessarily, be operatively focused by the focusing fluid. The focusing stream and the focused stream may preferably, but need not necessarily, operatively flow out from the outlet portion as a single flow stream.

According to an aspect of one preferred embodiment of the invention, the focusing stream may preferably, but need not necessarily, substantially surround the focused stream in the single flow stream.

According to an aspect of one preferred embodiment of the invention, the liquid-containing cell may preferably, but need not necessarily, be operatively sealed relative to the outside environment.

According to an aspect of one preferred embodiment of the invention, the flow focusing apparatus may preferably, but need not necessarily, operatively deliver the focused stream and the focusing stream, into intersection with one another, in the liquid-containing cell.

According to an aspect of one preferred embodiment of the invention, the system may preferably, but need not necessarily, also include a volume of a gas—preferably at a predetermined pressure, and preferably operatively contained within the liquid-containing cell.

According to an aspect of one preferred embodiment of the invention, the system may preferably, but need not necessarily, also include a gas pressure source. The liquid-containing cell may preferably, but need not necessarily, be shaped to define an inlet valve. The gas pressure source may preferably, but need not necessarily, operatively pressurize the gas—preferably via the inlet valve, and preferably in the liquid-containing cell.

According to an aspect of one preferred embodiment of the invention, the liquid-containing cell may preferably, but need not necessarily, be shaped to define a pressure safety valve. The pressure safety valve may preferably, but need not necessarily, operatively release a portion of the gas and/or the fluid bath—preferably, when the pressure exceeds a predetermined maximum safety pressure for the sealed liquid-containing cell.

According to an aspect of one preferred embodiment of the invention, the pressure safety valve may preferably, but need not necessarily, be provided on, and/or in operative fluid relation with, the outlet port of the liquid-containing cell. The pressure safety valve may preferably, but need not necessarily, operatively release a portion of the fluid bath, preferably when the pressure exceeds the predetermined maximum safety pressure.

According to an aspect of one preferred embodiment of the invention, the gas may preferably, but need not necessarily, include an inert gas.

According to an aspect of one preferred embodiment of the invention, (i) the pressure of the gas, and/or operative flow rates for (ii) the focused stream through the polymer nozzle and/or (iii) the focusing stream through the focusing nozzle, may preferably be predetermined—preferably in dependent relation upon one another, and preferably so as to maintain the fluid bath at a substantially constant liquid level.

According to an aspect of one preferred embodiment of the invention, the liquid-containing cell further may preferably, but need not necessarily, include a stirring bar. The stirring bar may preferably, but need not necessarily, operatively maintain the fluid bath under stirring. The fluid bath may preferably, but need not necessarily, operatively allow the microbeads to solidify.

According to an aspect of one preferred embodiment of the invention the stirring bar may preferably, but need not necessarily, include an electric stirring bar and/or a magnetic stirring bar.

According to an aspect of one preferred embodiment of the invention, the liquid-containing cell may preferably, but need not necessarily, be shaped to define a sealed orifice. The sealed orifice may preferably, but need not necessarily, be selectively openable—preferably so as to recover substantially solidified microbeads through the orifice, from the fluid bath.

According to an aspect of one preferred embodiment of the invention, the system may preferably, but need not necessarily, also include a conduit in fluid communication between the outlet port and the focusing nozzle—preferably, so as to operatively recycle at least part of the volume of the focusing fluid operatively delivered out from the fluid bath, preferably via the outlet port, and preferably as at least part of the focusing stream operatively delivered by the focusing nozzle.

According to an aspect of one preferred embodiment of the invention, the medium may preferably, but need not necessarily, include an organic solvent.

According to an aspect of one preferred embodiment of the invention, the organic solvent may preferably, but need not necessarily, include chloroform and/or dichloromethane.

According to an aspect of one preferred embodiment of the invention, the polymer may preferably, but need not necessarily, be substantially hydrophobic.

According to an aspect of one preferred embodiment of the invention, the polymer may preferably, but need not necessarily, include a polystyrene powder and/or a derivative thereof.

According to an aspect of one preferred embodiment of the invention, the focusing fluid may preferably, but need not necessarily, include water.

According to an aspect of one preferred embodiment of the invention, the polymer solution and/or suspension may preferably, but need not necessarily, also include particles dissolved and/or dispersed in the medium. Each of the microbeads may preferably, but need not necessarily, bind an identifiable set of the particles.

According to an aspect of one preferred embodiment of the invention, the particles may preferably, but need not necessarily, include fluorophores.

According to an aspect of one preferred embodiment of the invention, the particles may preferably, but need not necessarily, include nanoparticles.

According to an aspect of one preferred embodiment of the invention, the nanoparticles may preferably, but need not necessarily, include semiconductor nanoparticles, magnetic nanoparticles, metallic conductor nanoparticles, metal oxide nanoparticles, and/or fluorescent nanoparticles.

According to an aspect of one preferred embodiment of the invention, the particles may preferably, but need not necessarily, include quantum dots.

According to an aspect of one preferred embodiment of the invention, the particles may preferably, but need not necessarily, include a combination of quantum dots and/or magnetic nanoparticles.

According to an aspect of one preferred embodiment of the invention, the polymer solution and/or suspension may preferably, but need not necessarily, have a concentration of about 0.04 by weight-weight percentage (4 wt %).

According to the invention, there is disclosed still another system for forming one or more concentrated volumes of microbeads. The system is for use with a fluid bath, a focusing fluid, and/or a polymer solution and/or suspension. The polymer solution and/or suspension includes a polymer dissolved and/or dispersed in a medium. The system includes a flow focusing apparatus. The flow focusing apparatus includes a polymer nozzle and a focusing nozzle. The polymer nozzle operatively delivers a focused stream of the polymer solution and/or suspension. The focusing nozzle operatively delivers a focusing stream of the focusing solution. The flow focusing apparatus operatively delivers the focused stream and the focusing stream into intersection with one another. The flow focusing apparatus operatively flows the focusing stream and the focused stream into the fluid bath, so as to form the microbeads in the fluid bath. The system also includes a liquid-containing cell which is shaped to define an outlet port. The liquid-containing cell operatively contains the fluid bath and operatively delivers a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath.

To put it another way, the invention may be said to include a method of manufacturing polymer microspheres. This inventive method includes the steps of: (a) directing a focusing fluid through a focusing nozzle to create a focusing stream; (b) directing a polymer solution and/or suspension (or “focused fluid”) through a polymer nozzle to create a focused stream; (c) intersecting the focusing stream and the focused stream inside a liquid-containing cell—preferably, but not necessarily, below the liquid level in the cell—to form the microspheres. The concentration of the microspheres in the cell may preferably, but need not necessarily, be controlled by adjusting a volume of liquid in the cell.

According to an aspect of one preferred embodiment of the invention, the focused fluid may preferably, but need not necessarily, include a polymer solution and/or suspension. The focusing fluid may preferably, but need not necessarily, include water.

According to an aspect of one preferred embodiment, the invention also extends to a system for manufacturing polymer microspheres. The system includes a liquid-containing cell and a nozzle assembly. The nozzle assembly may preferably be positioned within the cell. The nozzle assembly may preferably include a focusing nozzle producing the focusing stream and a polymer nozzle (or “focused nozzle”) producing a stream of the focused fluid. The nozzles are preferably operative to intersect the focusing stream with the stream of the focused fluid, so as to form microspheres from the focused fluid.

Other advantages, features and/or characteristics of the present invention, as well as methods of operation and/or functions of the related elements of the method and system, and/or the combination of steps, parts and/or economies of manufacture, will become more apparent upon consideration of the following detailed description and the appended claims with reference to the accompanying drawings, the latter of which are briefly described hereinbelow.

BRIEF DESCRIPTION OF THE DRAWINGS

The novel features which are believed to be characteristic of the system and method according to the present invention, as to their structure, organization, use, and method of operation, together with further objectives and advantages thereof, will be better understood from the following drawings in which presently preferred embodiments of the invention will now be illustrated by way of example. It is expressly understood, however, that the drawings are for the purpose of illustration and description only, and are not intended as a definition of the limits of the invention. In the accompanying drawings:

FIG. 1 is a front view of a system for forming a concentrated volume of microbeads according to a preferred embodiment of the present invention;

FIG. 2 is an exploded view of the system shown in FIG. 1;

FIG. 3 is a sectional front view of a flow focusing apparatus of the system of FIG. 1, showing area 3A in phantom outline;

FIG. 3A is an enlarged view of area 3A from FIG. 3; and

FIG. 4 is an illustrative representation of a conjugated and bound microbead according to a preferred embodiment of the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Referring now to FIGS. 1-4, it will be appreciated that the inventive system and method presented herein may preferably include, or be used in conjunction with, a fluid bath 306, a focusing fluid 300, and a focused fluid (preferably, a polymer solution and/or suspension) 150.

As shown in FIG. 1, the system preferably includes a flow focusing apparatus 10 and a liquid-containing cell 100. The flow focusing apparatus 10 includes two fluid nozzles—i.e., a focused fluid nozzle (alternately referred to as a “polymer nozzle”) 20 and a focusing nozzle 30. Preferably, the polymer solution and/or suspension 150 is fed to the polymer nozzle 20. The focusing fluid 300 is fed to the focusing nozzle 30. The flow focusing apparatus 10 also includes a flow focusing body 40 which has an interior chamber 46—operatively, a locus for an intersection 154 of a focused stream 152 flowing from the polymer nozzle 20 and a focusing stream 302 flowing from the focusing nozzle 30.

The focusing fluid 300 in the focusing stream 302 is directed into contact with the focused stream (alternately, referred to as the “polymer stream”) 152 in the interior chamber 46 of the focusing body 40, so as to focus the polymer stream 152 toward an outlet portion 50 of the flow focusing body 40.

From the intersection 154 (and as best seen in FIG. 3A), the focused stream 152 and the focusing stream 302 flow as a single flow stream 402, through the outlet portion (or “pinhole”) 50, and out of the flow focusing body 40. The focusing fluid 300 (in the focusing stream 302) and the polymer stream 152 focused thereby flow, as the single flow stream 402, out from the interior chamber 46 and through the pinhole 50. At that point, the focusing stream 302 substantially surrounds the focused stream 152 in the single flow stream 402. The single flow stream 402 then flows out from the outlet portion 50 of the focusing body 40.

Pendant droplets 406 detach from a leading edge portion 404 of the single flow stream 402, so as to form microbeads 500 (still wet) which are surrounded by the focusing liquid 300 in the fluid bath 306.

One preferred embodiment of the present invention utilizes a polystyrene polymer solution and/or suspension as the focused fluid 150, and water as the focusing fluid 300. This preferred embodiment is suitable to create polystyrene microbeads 500.

The microbeads 500 are collected within the fluid bath 306 inside the liquid-containing cell 100. Subsequently, the microbeads 500 are solidified.

In a preferred embodiment according to the present invention, and as best seen in FIG. 1, the outlet portion 50 of the flow focusing body 40 is immersed in the fluid bath 306. Preferably, the fluid bath 306 also contains the focusing fluid 300—i.e., preferably, a water solution. The fluid bath 306 may preferably be maintained under stirring conditions (as described elsewhere herein) for the duration of the process of solidifying the microbeads 500. The microbeads 500 are preferably allowed to solidify before being recovered from the fluid bath 306.

The flow focusing apparatus 10 is incorporated into the liquid-containing cell 100, as shown in FIG. 1. The ends of the nozzles 20, 30 are within the cell 100. As such, the fluid streams 152, 302, 402 are emitted within the volume of the cell 100. The cell 100 is shown in more detail in FIG. 2.

The cell 100 includes a glass cylinder 200 sealed to an upper plate 210 and a lower plate 220 by o-rings 215 and 225, respectively. Although atmospheric pressure may preferably be sufficient to push the filtrate through a filter 235 and into filtrate port 230, additional pressure may be provided via a pressure inlet valve 260. As best seen in FIG. 1, the cell 100 may preferably be operatively sealed relative to the outside environment 98. The cell 100 may be pressurized via a gas pressure source 330 supplying a pressurized, preferably inert, gas 320 (e.g., nitrogen) through pressure inlet valve 260.

A pressure safety valve 232 may preferably be mounted on the filtrate port 230 (alternately, referred to as the outlet port 230), so as to help control the pressure within the cell 100, and so as to obviate (or reduce) any risk that the cell 100 might otherwise exceed a maximum pressure which the glass cylinder 200 is able to sustain. For some exemplary glass cylinders 200, the maximum pressure may typically be about 6 bar (90 psi).

Fluid inlet ports 120, 130 preferably supply the polymer solution and/or suspension 150 and the focusing fluid 300, respectively, into the cell 100 and to the nozzles 20, 30 as shown in FIG. 1. A first one of the fluid inlet ports 120 supplies the polymer solution and/or suspension 150 to the polymer nozzle 20, and a second one of the fluid inlet ports 130 supplies the focusing fluid 300 to the focusing nozzle 30.

A selectively openable orifice 250 allows the introduction of water into the fluid bath 306 in the cell 100. The flow focusing apparatus 10 is preferably immersed in the fluid bath 306. At the end of the process, suspended and solidified microbeads 500 may preferably be removed from the cell 100 through the orifice 250.

A stirring bar 240, either magnetic or electric, is preferably provided to stir the contents of the cell 100 for the duration μ of the process of solidifying the microbeads 500.

As best seen in FIG. 2, the cell 100 may be selectively assembled and/or disassembled by means of support posts 270 and screw knobs 275. Other assembly and disassembly methods previously known in the art may, however, be used in place thereof.

The size of the microbeads 500 formed according to the present invention may be dependent upon the flow rates in the nozzles 20, 30 and the concentration of the polymer used. The microbeads 500 are preferably retained (or trapped) within the cell 100 by the filter 235. A volume of the focusing fluid 300 (preferably, water) is preferably removed from the fluid bath 306, via the filtrate port 230. The filter type may be predetermined in dependent relation upon on the size of the microbeads 500 which are sought to be accumulated in the fluid bath 306.

The filter 235 may also be used to ensure, facilitate or increase the likelihood of monodispersity of the microbeads 500. (Though not shown in the drawings, it is contemplated that a series of increasingly fine filters 235 might be used to divide the microbeads 500 into a plurality of collections of differing monodispersity.) In these and other contemplated embodiments, there may exist some risk of one or more filters 235 becoming clogged, and/or of further purification of the focusing fluid 300 being required (e.g., before recycling the focusing fluid 300).

Example 1

To generate 6 μm polystyrene beads using the method and system described herein, a commercial polystyrene powder (offered by Sigma-Aldrich Canada Ltd. of Oakville, Ontario, Canada) was dissolved and/or dispersed into dichloromethane to create a 4% polymer solution and/or suspension. The resulting solution was then introduced into a commercial nozzle (i.e., an Avant-1™ nozzle offered by Ingeniatrics S.L. of Seville, Spain) using a syringe pump (i.e., a SP1001™ syringe pump offered by World Precision Instruments, Inc. of Sarasota, Fla., U.S.A.) at a rate of 1 mL/h, along with water as the focusing fluid 300, using a digital gear pump (offered by the Cole-Parmer Instrument Company of Vernon Hills, Ill., U.S.A.) at a rate of 180 mL/h. During the reaction, the nozzle inside the ultrafiltration cell was immersed into a 100 mL water solution under stirring. The volume of water solution used is dependent on the volume of the cell 100 and the location of the nozzle. Mixed cellulose ester filters 235 of 0.65 μm size (offered by the Millipore Corporation of Billerica, Mass., U.S.A.) were used. After synthesis, the filtrate port 230 was closed and suspended microbeads 500 were removed through the orifice 250.

Example 2

To create 5 μm polystyrene beads using the method and system described herein, a commercial polystyrene powder (offered by Sigma-Aldrich Canada Ltd. of Oakville, Ontario, Canada) was dissolved and/or dispersed into dichloromethane to create a 4% polymer solution and/or suspension. The resulting solution was then introduced into a commercial nozzle (i.e., an Avant-1™ nozzle offered by Ingeniatrics S.L. of Seville, Spain) using a syringe pump (i.e., a SP1001™ syringe pump offered by World Precision Instruments, Inc. of Sarasota, Fla., U.S.A.) at a rate of 0.5 mL/h, along with water as the focusing fluid 300, using a digital gear pump (offered by the Cole-Parmer Instrument Company of Vernon Hills, Ill., U.S.A.) at a rate of 180 mL/h. During the reaction, the nozzle inside the ultrafiltration cell was immersed into a 100 mL water solution under stirring. The volume of water solution used is dependent on the volume of the cell 100 and the location of the nozzle. Mixed cellulose ester filters 235 of 0.65 μm size (offered by the Millipore Corporation of Billerica, Mass., U.S.A.) were used. After synthesis, the filtrate port 230 is closed and suspended microbeads 500 are removed through the orifice 250.

By controlling a liquid level 310 within the cell 100 in accordance with the flow rates of the focused solution 150 and the focusing fluid 300, an equilibrium point may preferably be achieved. In this manner, and due in part to atmospheric pressure, the volume of the liquid suspension of the microbeads 500 in the cell 100 stays substantially constant over time. Excess focusing fluid 300 is filtered out. As such, the concentration of the microbeads 500 within the cell 100 increases. Accordingly, a higher concentration of the microbeads 500 may preferably be produced in a smaller volume of the fluid bath 306, preferably without the need for multiple centrifugations and/or for other concentration steps. Additionally, the extracted liquid can be recycled and fed back in as the focusing fluid 300, via a conduit 280 (best seen in FIGS. 1 and 2). In this way, the system and method according to the present invention may preferably help to reduce the need for large volumes of the focusing fluid 300 in large-scale production of microbeads 500.

For example, use of the present concentration-controlled flow focusing method and system to synthesize 5 μm microbeads over a period of 10 hours—using a 300 mL cell with the volume of the microbead suspension within the cell being kept at 100 mL—would produce about 5820 million microbeads at a concentration of about 0.4 wt %. The 100 mL suspension of microbeads may be further concentrated by splitting the volume into 2×50 mL Falcon tubes and centrifuging them. By contrast, over the same 10 hour period, prior art synthesis methods might produce roughly the same number of microbeads (i.e., about 5820 million microbeads), but at a concentration of only 0.02 wt % in a total volume of 1.9 L (1910 mL). To then concentrate this solution would require the use of 39×50 mL Falcon tubes. In this example, the present invention provides a microbead solution that is about 20 times more concentrated, over the same 10 hour period. Use of a smaller cell may be expected to yield even more concentrated bead solutions, perhaps up to 200 times that of the previous synthesis methods.

Referring now to FIG. 4, there is depicted a conjugate 800 including a microbead 500 produced according to a preferred embodiment of the present invention. The microbead 500 contains a set of particles 506—more particularly, a set 506 of two types of quantum dots 506A, 506B—encapsulated within the microbead 500. A surface 502 of the microbead 500 possesses functional groups 504 operatively bound with the biorecognition molecules 600 that are themselves operatively bound to target molecules 700 (e.g., markers for infections, diseases and/or genetic expression factors).

The identifiable set 506 of the quantum dots 506A, 506B may be adapted to, following irradiation, produce one or more identifiable spectral signals based on color and/or intensity.

Other modifications and alterations may be used in the design and manufacture of other embodiments according to the present invention without departing from the spirit and scope of the invention, which, is limited only by the accompanying claims of this application.

While the above preferred embodiments have been presented in the context of QDs, the method and system is equally applicable to other particle, including nanoparticles. Types of nanoparticles which are capable of being used in conjunction with the method and system according to the present invention may preferably include, but are not limited to, hard nanoparticles, polymer nanoparticles, magnetic nanoparticles, metallic conductor nanoparticles, metal oxide nanoparticles, fluorescent nanoparticles, and phosphorescent nanoparticles.

The foregoing description has been presented for the purpose of illustration and is not intended to be exhaustive or to limit the invention to the precise form disclosed. Many modifications and variations are possible in light of the above teaching and will be apparent to those skilled in the art. It is intended the scope of the invention be limited not by this description but by the claims. 

What is claimed is:
 1. A concentrated volume of microbeads, the concentrated volume of microbeads being formed according to a method comprising steps of: (a) flowing a focused stream of a polymer solution, polymer suspension, or polymer solution and suspension towards a fluid bath, with the polymer solution, polymer suspension, or polymer solution and suspension comprising a polymer dissolved, dispersed, or dissolved and dispersed in a medium; (b) flowing a focusing stream of a focusing fluid towards the fluid bath, and into intersection with the focused stream; (b.1) after step (b), maintaining the fluid bath under stirring; (c) flowing the focusing stream and the focused stream from intersection with one another, so as to form the microbeads in the fluid bath, and allowing the microbeads to solidify; and (d) flowing a volume of the focusing fluid from the fluid bath, so as to concentrate the microbeads in the fluid bath.
 2. A concentrated volume of microbeads according to claim 1, wherein one or more of the microbeads in the concentrated volume comprises one or more functional groups at a surface thereof, with the functional groups being adapted to operatively bind with biorecognition molecules.
 3. A concentrated volume of microbeads according to claim 2, wherein one or more of the microbeads in the concentrated volume, operatively bound with the biorecognition molecules, is adapted for use as a probe in a multiplexed diagnostic test for detection of one or more diseases.
 4. A concentrated volume of microbeads according to claim 3, wherein the diseases include malaria, HIV, Hepatitis B, Hepatitis C, Dengue virus, or avian flu (H5N1).
 5. A concentrated volume of microbeads according to claim 2, wherein one or more of the microbeads in the concentrated volume, operatively bound with the biorecognition molecules, is adapted for use as a probe in a multiplexed diagnostic test for detection of one or more genetic expression factors.
 6. A system for forming one or more concentrated volumes of microbeads, the system comprising: (e) a fluid bath, a focusing fluid, and a polymer solution, polymer suspension, or polymer solution and suspension comprising a polymer dissolved, dispersed, or dissolved and dispersed in a medium; (f) a flow focusing apparatus comprising: (i) a polymer nozzle operatively delivering a focused stream of the polymer solution, polymer suspension, or polymer solution and suspension; and (ii) a focusing nozzle operatively delivering a focusing stream of the focusing solution; with the flow focusing apparatus operatively delivering the focused stream and the focusing stream into intersection with one another, and with the flow focusing apparatus operatively flowing the focusing stream and the focused stream into the fluid bath, so as to faun the microbeads in the fluid bath; and (g) a liquid-containing cell shaped to define an outlet port, with the liquid-containing cell operatively containing the fluid bath and operatively delivering a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath; wherein the liquid-containing cell further comprises a stirring bar operatively maintaining the fluid bath under stirring, and wherein the fluid bath operatively allows the microbeads to solidify.
 7. The system according to claim 6, wherein operative flow rates for (i) the focused stream through the polymer nozzle, (ii) the focusing stream through the focusing nozzle, and (iii) the focusing fluid through the outlet port, respectively, are predetermined in dependent relation upon one another, so as to maintain the fluid bath at a substantially constant liquid level.
 8. The system according to claim 6, wherein the liquid-containing cell comprises one or more filters on the outlet port, with the volume of the focusing fluid being operatively delivered, through the filters, out from the fluid bath.
 9. The system according to claim 8, wherein the filters operatively retain the microbeads in the fluid bath.
 10. The system according to claim 8, wherein the filters operatively retain a substantially monodisperse set of the microbeads in the fluid bath.
 11. The system according to claim 8, wherein the filters operatively divide the microbeads into one or more collections of microbeads, with each of the collections including a respectively monodisperse set of the microbeads.
 12. The system according to claim 6, wherein the flow focusing apparatus further comprises a flow focusing body defining an interior chamber and an outlet portion, with the focused stream and the focusing stream being operatively delivered into intersection with one another in the chamber, and with the focusing stream and the focused stream operatively flowing out from the outlet portion of the flow focusing body.
 13. The system according to claim 12, wherein the outlet portion of the flow focusing body is operatively located below a liquid level of the fluid bath.
 14. The system according to claim 12, wherein the focused stream is operatively focused by the focusing fluid, and wherein the focusing stream and the focused stream operatively flow out from the outlet portion as a single flow stream.
 15. The system according to claim 14, wherein the focusing stream substantially surrounds the focused stream in the single flow stream.
 16. The system according to claim 6, wherein the liquid-containing cell is operatively sealed relative to the outside environment.
 17. The system according to claim 16, wherein the flow focusing apparatus operatively delivers the focused stream and the focusing stream, into intersection with one another, in the liquid-containing cell.
 18. The system according to claim 16, further comprising a volume of a gas at a predetermined pressure, operatively contained within the liquid-containing cell.
 19. The system according to claim 18, further comprising a gas pressure source, wherein the liquid-containing cell is shaped to define an inlet valve, and wherein the gas pressure source operatively pressurizes the gas, via the inlet valve, in the liquid-containing cell.
 20. The system according to claim 18, wherein the liquid-containing cell is shaped to define a pressure safety valve, and wherein the pressure safety valve operatively releases a portion of the gas or the fluid bath, when the pressure exceeds a predetermined maximum safety pressure for the sealed liquid-containing cell.
 21. The system according to claim 20, wherein the pressure safety valve is provided on, and in operative fluid relation with, the outlet port of the liquid-containing cell, and wherein the pressure safety valve operatively releases a portion of the fluid bath, when the pressure exceeds the predetermined maximum safety pressure.
 22. The system according to claim 19, wherein the gas comprises an inert gas.
 23. The system according to claim 19, wherein (i) the pressure of the gas is predetermined, in balance with operative flow rates for (ii) the focused stream through the polymer nozzle and (iii) the focusing stream through the focusing nozzle, so as to maintain the fluid bath at a substantially constant liquid level.
 24. The system according to claim 6, wherein the stirring bar comprises an electric stirring bar or a magnetic stirring bar.
 25. The system according to claim 6, wherein the liquid-containing cell is shaped to define a sealed orifice, with the sealed orifice being selectively openable, so as to recover solidified microbeads through the orifice, from the fluid bath.
 26. A system for foaming one or more concentrated volumes of microbeads, the system comprising: (a) a fluid bath, a focusing fluid, and a polymer solution, polymer suspension, or polymer solution and suspension comprising a polymer dissolved, dispersed, or dissolved and dispersed in a medium; (b) a flow focusing apparatus comprising: (i) a polymer nozzle operatively delivering a focused stream of the polymer solution, polymer suspension, or polymer solution and suspension; and (ii) a focusing nozzle operatively delivering a focusing stream of the focusing solution; with the flow focusing apparatus operatively delivering the focused stream and the focusing stream into intersection with one another, and with the flow focusing apparatus operatively flowing the focusing stream and the focused stream into the fluid bath, so as to faun the microbeads in the fluid bath; (c) a liquid-containing cell shaped to define an outlet port, with the liquid-containing cell operatively containing the fluid bath and operatively delivering a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath; and (d) a conduit in fluid communication between the outlet port and the focusing nozzle, so as to operatively recycle at least part of the volume of the focusing fluid operatively delivered out from the fluid bath, via the outlet port, as at least part of the focusing stream operatively delivered by the focusing nozzle.
 27. The system according to claim 6, wherein the medium comprises an organic solvent.
 28. The system according to claim 26, wherein the organic solvent comprises chloroform or dichloromethane.
 29. The system according to claim 6, wherein the polymer is substantially hydrophobic.
 30. The system according to claim 6, wherein the polymer comprises a polystyrene powder or a derivative thereof.
 31. The system according to claim 6, wherein the focusing fluid comprises water.
 32. The system according to claim 6, wherein the polymer solution, polymer suspension, or polymer solution and suspension further comprises particles dissolved, dispersed, or dissolved and dispersed in the medium, and wherein each of the microbeads binds an identifiable set of the particles.
 33. The system according to claim 32, wherein the particles comprise fluorophores.
 34. The system according to claim 32, wherein the particles comprise nanoparticles.
 35. The system according to claim 34, wherein the nanoparticles comprise semiconductor nanoparticles, magnetic nanoparticles, metallic conductor nanoparticles, metal oxide nanoparticles, fluorescent nanoparticles, or phosphorescent nanoparticles.
 36. The system according to claim 32, wherein the particles comprise quantum dots.
 37. The system according to claim 32, wherein the particles comprise a combination of quantum dots and magnetic nanoparticles.
 38. The system according to claim 6, wherein the polymer solution, polymer suspension, or polymer solution and suspension has a concentration of about 0.04 by weight-weight percentage (4 wt %).
 39. A system for forming one or more concentrated volumes of microbeads, the system being for use with a fluid bath, a focusing fluid, and a polymer solution, polymer suspension, or polymer solution and suspension comprising a polymer dissolved, dispersed, or dissolved and dispersed in a medium, the system comprising: (h) a flow focusing apparatus comprising: (i) a polymer nozzle operatively delivering a focused stream of the polymer solution, polymer suspension, or polymer solution and suspension; and (ii) a focusing nozzle operatively delivering a focusing stream of the focusing solution; with the flow focusing apparatus operatively delivering the focused stream and the focusing stream into intersection with one another, and with the flow focusing apparatus operatively flowing the focusing stream and the focused stream into the fluid bath, so as to form the microbeads in the fluid bath; and (i) a liquid-containing cell shaped to define an outlet port, with the liquid-containing cell operatively containing the fluid bath and operatively delivering a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath; wherein the liquid-containing cell further comprises stirring bar operatively maintaining the fluid bath under stirring, and wherein the fluid bath operatively allows the microbeads to solidify.
 40. A system for fowling one or more concentrated volumes of microbeads, the system being for use with a fluid bath, a focusing fluid, and a polymer solution, polymer suspension, or polymer solution and suspension comprising a polymer dissolved, dispersed, or dissolved and dispersed in a medium, the system comprising: (a) a flow focusing apparatus comprising: (i) a polymer nozzle operatively delivering a focused stream of the polymer solution, polymer suspension, or polymer solution and suspension; and (ii) a focusing nozzle operatively delivering a focusing stream of the focusing solution; with the flow focusing apparatus operatively delivering the focused stream and the focusing stream into intersection with one another, and with the flow focusing apparatus operatively flowing the focusing stream and the focused stream into the fluid bath, so as to form the microbeads in the fluid bath; (b) a liquid-containing cell shaped to define an outlet port, with the liquid-containing cell operatively containing the fluid bath and operatively delivering a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath; and (c) a conduit in fluid communication between the outlet port and the focusing nozzle, so as to operatively recycle at least part of the volume of the focusing fluid operatively delivered out from the fluid bath, via the outlet port, as at least part of the focusing stream operatively delivered by the focusing nozzle. 